Colon Cancer: Gene >> GPR161

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168104582:168104582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758001918
CDS Mutation	c.269G>A
AA Mutation	p.Arg90His(p.R90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168104775:168104775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373776672
CDS Mutation	c.76G>A
AA Mutation	p.Val26Ile(p.V26I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168085786:168085786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335G>T
AA Mutation	p.Lys445Asn(p.K445N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168104545:168104545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>A
AA Mutation	p.Phe102Leu(p.F102L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168104797:168104797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54G>T
AA Mutation	p.Glu18Asp(p.E18D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168087695:168087695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214T>C
AA Mutation	p.Met405Thr(p.M405T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168096612:168096612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779202531
CDS Mutation	c.995G>A
AA Mutation	p.Arg332His(p.R332H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168104496:168104496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781504641
CDS Mutation	c.355G>A
AA Mutation	p.Gly119Arg(p.G119R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367835
Start	168090598:168090598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771035075
CDS Mutation	c.1170G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367835
Start	168096968:168096968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759899756
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367835
Start	168097127:168097127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367835
Start	168085631:168085631(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1490delG
AA Mutation	p.Gly497AlafsTer13(p.G497Afs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GPR161

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168096969:168096969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767649249
CDS Mutation	c.638G>A
AA Mutation	p.Arg213His(p.R213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367835
Start	168096603:168096603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004T>G
AA Mutation	p.Leu335Arg(p.L335R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367835
Start	168097184:168097184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367835
Start	168104656:168104656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781674595
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367835
Start	168096527:168096527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000367835
Start	168096607:168096607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000G>T
AA Mutation	p.Glu334Ter(p.E334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript